A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16955243



Internal ID37471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:127095146..127095197hg38UCSC Ensembl
chr4:128016301..128016352hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5403580
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16955243
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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